FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇭 Switzerland
Invia Foam Dressing Kits with FitPad, Invia Foam Dressing Kits with FitPad, Invia Gauze Dressing Kits with FitPad, Invia FitPad, Invia Transparent Film
K Number: K170088
·
Decision Apr 6, 2017
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
204
Applicant Total
2
Review Days
86
Basic Information
- Device Name
- Invia Foam Dressing Kits with FitPad, Invia Foam Dressing Kits with FitPad, Invia Gauze Dressing Kits with FitPad, Invia FitPad, Invia Transparent Film
- K Number
- K170088
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4780
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- MEDELA, AG
- Date Received
- January 10, 2017
- Decision Date
- April 6, 2017
- Product Code
- OMP
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| OMP | Negative Pressure Wound Therapy Powered Suction Pump | FDA class 2 | General, Plastic Surgery |
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Other Clearances by MEDELA, AG
| K Number | Device Name | ||
|---|---|---|---|
| K142626 | Invia Liberty Negative Pressure Wound Therapy System, Invia Liberty Tubing Set, Y-connector, Drain Adaptor, Invia Liberty Canisters | Jun 12, 2015 | Substantially Equivalent |